FINDING 2024‐001 – Allowable Cost Principles and Activities Allowed or Unallowed Material Weakness in Internal Control over Compliance Assistance Listing Number: 21.029 Federal Program Name: COVID-19 - Coronavirus Capital Projects Fund Award Year: 2024 Criteria: Uniform Guidance requires non-Federal entities to establish and maintain effective internal controls over Federal awards, including ensuring transactions are properly recorded, reported, and allowable. Specifically: • 2 CFR §200.302(b)(1) and (b)(2) require financial management systems to provide accurate, current, and complete disclosure of financial results and to identify expenditures by Federal award. • 2 CFR §200.302(b)(6) requires written procedures for determining the allowability of costs. • 2 CFR §200.303 requires entities to establish and maintain effective internal controls over compliance, including appropriate segregation of duties. Condition and context: The Cooperative does not have formalized written policies and procedures governing the coding, review, and reporting of expenditures charged to Federal awards, including payroll costs. Additionally, adequate segregation of duties is not in place over the review and approval of expenditure coding and financial reporting. As a result, payroll expenditures were not consistently or timely coded to the appropriate grant. Payroll expenditures totaling $16,990 were identified subsequent to year-end and recorded and reported late. These costs were not included in the appropriate reporting period, resulting in delayed recognition of allowable expenditures. Questioned costs: None. Effect: The absence of formal policies, procedures, and proper segregation of duties increases the risk that expenditures are not accurately, completely, or timely recorded and reported by Federal award. This may result in: • Financial reports that do not reflect complete and accurate program expenditures for the reporting period; • Increased risk of noncompliance with Federal reporting requirements; • Potential misstatement or omission of allowable costs; and • Delays in reimbursement or increased risk of questioned costs. Additionally, the late identification and backdating of payroll expenditures contributed to the triggering of Single Audit requirements, which are now being performed after the required timeframe. Cause: The deficiencies are due to a lack of formalized written policies and procedures over expenditure coding, allowability determinations, and reporting, as well as inadequate segregation of duties in the preparation, review, and approval of grant-related expenditures and reports. Repeat finding: No Recommendation: We recommend the Cooperative develop and implement written policies and procedures to ensure timely, consistent, and correct coding of all grant-related expenditures (payroll and non-payroll). Within these policies and procedures, we recommend establishing review and approval controls, including periodic review of expenditure coding by supervisory or accounting personnel. Implementing these policies and procedures will ensure expenditures are recorded within the appropriate reporting period. Views of responsible officials and planned corrective actions: Wabash currently maintains informal procedures for coding and reviewing invoices and payroll records, management recognizes the need for a formalized, written policy governing expenditures charged to federal awards. To address identified material weaknesses, Wabash is committed to implementing a comprehensive written policy by June 30, 2026. This policy will formalize the coding, review, and reporting processes for all federal expenditures. Contact Person(s): Cheryl Gaither, Controller Justin Gephart, Chief Operating Officer
Finding No. 2024-001 Implement System-Based Tracking of Federal Expenditures Assistance Listing Number: 93.566 Program Name: Refugee and Entrant Assistance State/Replacement Designee Administered Programs Federal Agency: Department of Health and Human Services (HHS) Passed Through Entities: 1. California Department of Social Services 2. University of California, San Diego 3. California Rural Legal Assistance Foundation 4. San Diego Refugee Communities Coalition/United Women of East Africa Support Team 5. Public Health Institute (PHI) Federal Award Numbers: ALSP22-0002-A1, ALSP23-0001, PUR00533092, ACS22-05-CAIR, 06568-AR76924 Federal Award Year: August 1, 2022 to June 30, 2026 Compliance Requirement: Activities Allowed or Unallowed Criteria: Management is responsible for designing, implementing, and maintaining an internal control system that ensures accurate financial reporting. Effective internal control over financial reporting provides reasonable assurance regarding the completeness and accuracy of accounting records, and compliance with grantor requirements. 2 CFR 200.510 Financial Statements require auditees to prepare a Schedule of Expenditures of Federal Awards (SEFA) for the period covered by the auditee's financial statements. This schedule must include the total Federal awards expended, as determined in accordance with 2 CFR 200.502. The information presented should be consistent with the accounting records (i.e., general ledger). In addition, Section 2 CFR 200.302(b)(1) provides that non-Federal entities must maintain effective control over and accountability for all funds, and must identify, in their accounts, all Federal awards received and expended. Condition: During our review of the SEFA, we noted that CAIR-CA utilizes workbooks outside of its accounting software to track federal expenditures. The workbooks do not reconcile directly with the general ledger (GL), so management performs a separate reconciliation to support the SEFA amounts. This approach was similarly observed in the prior year's audit. Cause: The prior year audit was completed in August 2025, after the close of the fiscal year 2024. As a result, management was still in the process of implementing a system-based tracking during the year 2024. CAIR-CA’s processes for tracking federal awards are continuing to develop, as this is only the second year under Single Audit. Effect: Using manual workbooks requires additional manual effort and may make reconciliation between SEFA and GL more time-consuming, and may result in inaccurate or incomplete reporting. Questioned Cost: None Recommendation: We recommend that CAIR-CA continue enhancing its accounting processes to track federal expenditures directly within its accounting software. This could include GL tracking codes or other similar identifiers for federal programs. System based tracking would simplify SEFA preparation, improve consistency with the general ledger, and strengthen monitoring of federal expenditures. Views of Responsible Officials and Corrective Action Plan: Management concurs with the finding and has already updated the accounting system to incorporate grant-specific tracking codes to further align with federal reporting standards. Because the organization’s first single audit in FY2023 was conducted concurrently with the FY2024 single audit, there was limited opportunity for these procedural improvements to be reflected in the FY2024 single audit testing cycle. As a result, the impact of these changes will be more fully reflected in the FY2025 single audit, which is scheduled to commence this year. As part of a layered approach to internal controls, excel worksheets will continue to be used as a supplementary monitoring tool, providing an additional cross-check to the system-generated reports. Responsible person: Jackie Ramirez, Operations & Finance Associate Director Implementation date: November 20, 2025
Criteria: Per 2 CFR § 200.303(a), the non-Federal entity must establish, document, and maintain effective internal control over Federal awards that provides reasonable assurance that the entity is managing the award in compliance with Federal statutes, regulations, and the terms and conditions of the awards. Additionally, per 2 CFR §200.403 and §200.302, costs charged to federal awards must be allowable, allocable, and properly documented, and financial reporting must be accurate, complete, and supported by the accounting system. Condition: Although the Parish has implemented internal controls related to the allowability of costs and the preparation of required reports for the Coronavirus State and Local Fiscal Recovery funds, they were not operating effectively during fiscal year 2024. Tests of controls indicated that transactions were not tracked appropriately to ensure they were charged to the correct funding source. In addition, quarterly project and expenditure reports submitted to the U.S. Treasury included inaccurate or unsupported information due to a lack of tracking and reconciliation procedures. Cause: As discussed in item 2024-001, the Parish encountered several challenges during the transition of administration and key personnel. Parish administration and management were immediately tasked with enhancing operations related to procedural concerns from the prior administration and performing the accounting function without sufficient documentation on several balances and transactions. The documented controls were not in practice because of this. Effect: While no instances of noncompliance were noted, the lack of documented controls in practice increases the risk that future required reports could be incomplete, inaccurate, or untimely, as well as, federal costs being unallowed per the cost principles which could potentially result in program noncompliance. Recommendation: We recommend that the Parish enhance and document internal controls over financial reporting, as described in our recommendations described under item 2024-001, to prevent noncompliance of the Uniform Guidance as required. Views of responsible officials: See management’s responses to findings on Page 116.
Finding 2024-001, Expense Allocations - Financial Management (Assistance Listings 19.510, 93.566, 93.583 and 93.576) Criteria: Per 2 CFR § 200.302(a) (Financial Management), all recipient and subrecipient financial management systems must be sufficient to track expenditures and establish that funds have been used in accordance with federal statutes, regulations, and the terms and conditions of the federal award. Condition and Context: The Organization’s documentation related to the reconciliation of government grant revenue claimed and received to the actual revenue earned were not maintained. The lack of regular reconciliations increased the risk of misstatements in the financial records and delayed the financial reporting process. Cause: Internal controls over government grant revenue were not operating efficiently or designed properly. Effect: This resulted to significant amount of time required by both Management and the Auditors in order to analyze and adjust grant revenue, accounts receivables and deferred revenue balances accurately. Identification as a Repeat Finding: Yes. Questioned Costs: None. Recommendation: We recommend that the Organization strengthen its policies and procedures for reconciling the grant revenue earned to the related expenses. Financial reports and claims should be created from the reconciled general ledger. Additionally, management should establish clear documentation procedures to support the proper allocation of expenses in the general ledger and ensure compliance with federal regulations. View of responsible officials: Management has reviewed the finding and recommendations. We note that this item was identified as a repeat issue primarily due to the timing of the prior year's audit. Because the FY23 findings were delivered after FY24 had already concluded, the Organization did not have the opportunity to incorporate the auditors' feedback during the FY24 audited period. However, the Organization took immediate, proactive steps to deploy enhanced internal controls for FY25 to ensure continuous alignment with federal standards. To ensure strict adherence to 2 CFR § 200.302(a), we are actively implementing a more regular reconciliation process between government grant revenue claimed and actual revenue earned. As a key part of this initiative, the Organization has developed and deployed new internal financial tools designed to incorporate automation into our daily workflows. By utilizing these automated tools-such as standardized templates for recording cash receipts and systematically clearing Accounts Receivable-we have significantly enhanced the accuracy of our data entries and reduced the risk of manual misstatements. Our ongoing objective is to leverage these tools to establish clear, standardized documentation procedures, ensuring that all financial reports and claims are consistently generated from a reconciled general ledger. Management remains fully committed to dedicating the necessary time and resources to mature these financial controls and ensure robust compliance with federal regulations.
2 CFR § 1000.10 gives regulatory effect to the Department of Treasury for the following sections of 2 CFR 200: 2 CFR § 200.302(b)(7) requires written procedures for determining the allowability of costs in accordance with Subpart E-Cost Principles of this part and the terms and conditions of the Federal award. 2 CFR 200.320(b)(2)(ii) requires non-federal entities to have a written method for conducting technical evaluations of the competitive proposals received and for selecting contract recipients. 2 CFR 200.319(d) requires non-federal entities to have written procedures for procurement transactions to ensure all solicitations incorporate a clear and accurate description of the technical requirements for the property, equipment, or service to be procured and identify all requirements which the offerors must fulfill and all other factors to be used in evaluating bids or proposals. The Village was awarded grant monies under the Uniform Guidance (UG); however, the Village did not establish formal written policies required by the UG for the sections listed above. A lack of policies could result in inadequate guidance for individuals to follow and ensure proper compliance. To help ensure compliance with the Uniform Guidance requirements, the Village should establish and maintain timely updated policies and, more importantly, implement procedures as specified by UG requirements for all grant monies received. Any changes to the Village's policies should also be formally approved by Council and documented within the minutes.
2024-005 Internal Controls over Grant Management (Significant Deficiency and Noncompliance) (repeat finding 2023-005) Criteria: 2 CFR 200.302 establishes the requirements of a financial management system adequate to ensure compliance with federal regulations. This system must include written procedures to implement requirements for payment methods and determine the allowability of costs in accordance with subpart E. Statement of Condition: The City has written fiscal policies but they do not meet the financial management system requirements established in the regulations. Cause: The City has processes and procedures in place to administer grant funds but written policies do not contain compliance requirements. Effect: The City is not in compliance with financial management system requirements. Recommendation: The City should develop a grants manual or additional written policies to incorporate all the requirements of 2 CFR 200 and ensure compliance. Views of Management and Planned Corrective Action: See Corrective Action Plan included at the end of the report.
Finding 2024-005 Allowable Costs–Payroll Costs (Significant Deficiency and Noncompliance) (Repeat Finding) Information on the Federal Program: U.S. Department of Health and Human Services, Assistance Listing #93.243 Substance Abuse and Mental Health Services Projects of Regional and National Significance. Criteria: 2 CFR section 200.302 establishes the requirements for sufficient financial management over grant funding to ensure records adequately identify the source and application of funds for federally funded activities. These records must contain information pertaining to Federal awards, authorizations, financial obligations, unobligated balances, assets, expenditures, income and interest and be supported by source documentation. Condition: We tested 32 payroll disbursements across five pay periods. Of those 32, 5 exceptions were noted. One exception was that the amount of time and corresponding amounts allocated to the grant did not agree to the percentage documented on the employee’s timesheet. For the other 4 exceptions, the supporting time sheets could not be provided for a pay period tested. Cause: Employee timesheets are turned in after payroll is processed and allocations made, the timesheet in this exception did not agree to the amount allocated. Four supporting time sheets for a January payroll processed could not be located. Effect: The Council did not retain proper documentation to support payroll costs charged to the grant. Questioned Costs: $729 Recommendation: We recommend the Council strengthen procedures surrounding payroll so that the source documentation agrees to and is retained to support the amounts being allocated to the grant based on actual employee time. Views of Responsible Officials: See Management’s View and Corrective Action Plan at the end of the report.
Finding 2024-005 Allowable Costs–Payroll Costs (Significant Deficiency and Noncompliance) (Repeat Finding) Information on the Federal Program: U.S. Department of Health and Human Services, Assistance Listing #93.243 Substance Abuse and Mental Health Services Projects of Regional and National Significance. Criteria: 2 CFR section 200.302 establishes the requirements for sufficient financial management over grant funding to ensure records adequately identify the source and application of funds for federally funded activities. These records must contain information pertaining to Federal awards, authorizations, financial obligations, unobligated balances, assets, expenditures, income and interest and be supported by source documentation. Condition: We tested 32 payroll disbursements across five pay periods. Of those 32, 5 exceptions were noted. One exception was that the amount of time and corresponding amounts allocated to the grant did not agree to the percentage documented on the employee’s timesheet. For the other 4 exceptions, the supporting time sheets could not be provided for a pay period tested. Cause: Employee timesheets are turned in after payroll is processed and allocations made, the timesheet in this exception did not agree to the amount allocated. Four supporting time sheets for a January payroll processed could not be located. Effect: The Council did not retain proper documentation to support payroll costs charged to the grant. Questioned Costs: $729 Recommendation: We recommend the Council strengthen procedures surrounding payroll so that the source documentation agrees to and is retained to support the amounts being allocated to the grant based on actual employee time. Views of Responsible Officials: See Management’s View and Corrective Action Plan at the end of the report.
Finding 2024-005 Allowable Costs–Payroll Costs (Significant Deficiency and Noncompliance) (Repeat Finding) Information on the Federal Program: U.S. Department of Health and Human Services, Assistance Listing #93.243 Substance Abuse and Mental Health Services Projects of Regional and National Significance. Criteria: 2 CFR section 200.302 establishes the requirements for sufficient financial management over grant funding to ensure records adequately identify the source and application of funds for federally funded activities. These records must contain information pertaining to Federal awards, authorizations, financial obligations, unobligated balances, assets, expenditures, income and interest and be supported by source documentation. Condition: We tested 32 payroll disbursements across five pay periods. Of those 32, 5 exceptions were noted. One exception was that the amount of time and corresponding amounts allocated to the grant did not agree to the percentage documented on the employee’s timesheet. For the other 4 exceptions, the supporting time sheets could not be provided for a pay period tested. Cause: Employee timesheets are turned in after payroll is processed and allocations made, the timesheet in this exception did not agree to the amount allocated. Four supporting time sheets for a January payroll processed could not be located. Effect: The Council did not retain proper documentation to support payroll costs charged to the grant. Questioned Costs: $729 Recommendation: We recommend the Council strengthen procedures surrounding payroll so that the source documentation agrees to and is retained to support the amounts being allocated to the grant based on actual employee time. Views of Responsible Officials: See Management’s View and Corrective Action Plan at the end of the report.
Finding 2024-005 Allowable Costs–Payroll Costs (Significant Deficiency and Noncompliance) (Repeat Finding) Information on the Federal Program: U.S. Department of Health and Human Services, Assistance Listing #93.243 Substance Abuse and Mental Health Services Projects of Regional and National Significance. Criteria: 2 CFR section 200.302 establishes the requirements for sufficient financial management over grant funding to ensure records adequately identify the source and application of funds for federally funded activities. These records must contain information pertaining to Federal awards, authorizations, financial obligations, unobligated balances, assets, expenditures, income and interest and be supported by source documentation. Condition: We tested 32 payroll disbursements across five pay periods. Of those 32, 5 exceptions were noted. One exception was that the amount of time and corresponding amounts allocated to the grant did not agree to the percentage documented on the employee’s timesheet. For the other 4 exceptions, the supporting time sheets could not be provided for a pay period tested. Cause: Employee timesheets are turned in after payroll is processed and allocations made, the timesheet in this exception did not agree to the amount allocated. Four supporting time sheets for a January payroll processed could not be located. Effect: The Council did not retain proper documentation to support payroll costs charged to the grant. Questioned Costs: $729 Recommendation: We recommend the Council strengthen procedures surrounding payroll so that the source documentation agrees to and is retained to support the amounts being allocated to the grant based on actual employee time. Views of Responsible Officials: See Management’s View and Corrective Action Plan at the end of the report.
Finding 2024-005 Allowable Costs–Payroll Costs (Significant Deficiency and Noncompliance) (Repeat Finding) Information on the Federal Program: U.S. Department of Health and Human Services, Assistance Listing #93.243 Substance Abuse and Mental Health Services Projects of Regional and National Significance. Criteria: 2 CFR section 200.302 establishes the requirements for sufficient financial management over grant funding to ensure records adequately identify the source and application of funds for federally funded activities. These records must contain information pertaining to Federal awards, authorizations, financial obligations, unobligated balances, assets, expenditures, income and interest and be supported by source documentation. Condition: We tested 32 payroll disbursements across five pay periods. Of those 32, 5 exceptions were noted. One exception was that the amount of time and corresponding amounts allocated to the grant did not agree to the percentage documented on the employee’s timesheet. For the other 4 exceptions, the supporting time sheets could not be provided for a pay period tested. Cause: Employee timesheets are turned in after payroll is processed and allocations made, the timesheet in this exception did not agree to the amount allocated. Four supporting time sheets for a January payroll processed could not be located. Effect: The Council did not retain proper documentation to support payroll costs charged to the grant. Questioned Costs: $729 Recommendation: We recommend the Council strengthen procedures surrounding payroll so that the source documentation agrees to and is retained to support the amounts being allocated to the grant based on actual employee time. Views of Responsible Officials: See Management’s View and Corrective Action Plan at the end of the report.
Finding 2024-006 – Activities Allowed (Significant Deficiency and Noncompliance)(Repeat Finding) Information on the Federal Program: U.S. Department of Veterans Affairs, Assistance Listing #64.055 Staff Sergeant Parker Gordon Fox Suicide Prevention Grant Program. Criteria: 2 CFR section 200.302 establishes the requirements for sufficient financial management over grant funding to ensure funds have been used in accordance with Federal statues, regulations, and terms and conditions of the Federal award. These requirements include that the nonfederal entity compare expenditures with the approved award budget. Condition: We tested 22 nonpayroll disbursements; one of those expenses did not fit into an expense category in the approved award budget. Cause: The Council began allocating non-reimbursable expenses to their grant codes to track the true costs of running a program. This grant allowed for indirect costs; however, these costs were charged directly to the grant and were included in the amount requested for reimbursement and also in the cost base used for the indirect cost calculation. These costs were not in line with the categories of expenses in the award budget. Effect: The Council allocated costs that were not allowable activities per the grant budget. Questioned Costs: $255 Recommendation: We recommend the Council strengthen procedures over costs invoiced for reimbursement to ensure those costs are compared to the grant budget for allowability. Views of Responsible Officials: See Management’s View and Corrective Action Plan at the end of the report.
Item 2024-001 Uniform Guidance Written Policies, Procedures and Standards of Conduct U.S. Department of Treasury COVID-19 Coronavirus State and Local Fiscal Recovery Funds Listing #21.027 Year Ended September 30, 2024 Criteria – Grantees should have written policies, procedures, and standards of conduct as required by 2 CFR 200, Subparts D & E of the Uniform Guidance. 2 CFR 200, Subparts D & E requires the non-Federal entity to establish and maintain written policies, procedures, and standards of conduct including internal controls over the Federal awards that provides reasonable assurance that the non‐Federal entity is managing the Federal statutes, regulations, and the terms and conditions of the Federal award. Specific requirements relate to the following: • § 200.302 Financial management • § 200.305 Payment Condition – The City does not have written policies, procedures and standards of conduct. Cause – The entity has failed to prepare written policies, procedures, and standards of conduct as required by 2 CFR 200, Subparts D & E of the Uniform Guidance. Questioned Costs – None noted Effect – Lack of written policies, procedures, and standards of conduct could result in noncompliance related to federal awards. Recommendation – We recommend that the Commission prepare written policies, procedures, and standards of conduct to include all the required elements as provided in 2 CFR 200, Subparts D & E of the Uniform Guidance. Management’s Response – The City is evaluating the auditor’s recommendations and will implement the necessary corrective action based on a cost benefit analysis.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.
Finding 2024-001—Significant Deficiency in Internal Controls over Compliance: Research and Development Cluster Program—Research and Development Cluster (R&D) Criteria—Compliance with the financial management and internal control requirements outlined in Title 2 U.S. Code of Federal Regulations (CFR) Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards; Sections 200.302-303 (“Section 200.302-303”) is required for all federal awards. Section 200.302-303 outlines the various requirements around documentation and internal controls. Condition and Context—Baystate Health’s internal controls over R&D allowable costs, special tests and provisions, and subrecipient monitoring in accordance with Section 200.302-303 were not appropriately designed and implemented or operated effectively. Specifically, during the 2024 audit, the following conditions were identified: • In instances, controls, as described below, exhibited the following: o Certain roles and responsibilities within the Sponsored Programs Administration (SPA) were inadequately defined and not understood by control owners o inconsistent documentation evidencing review over R&D compliance requirements o lack of a central repository for documentation related to the performance of internal control procedures and compliance with grant requirements o ineffective review of key personnel labor distributions o Insufficient internal review of grant budgets concerning the indirect cost rate and salary cap authorized for individual federal awards • The testing of internal controls over subrecipient monitoring identified an absence of underlying documentation. For three out of nine subrecipient selections there were no records maintained to document the completion and outcomes of the subrecipient risk assessment. For nine out of nine subrecipient selections there was no documentation retained evidencing Baystate Health’s review of subrecipient’s most recent audit information, or of Baystate Health’s review of the subrecipients’ compliance with registration, suspension and debarment requirements. • Testing of annual salary distribution requirements for key personnel documentation identified three out of 60 selections where the records were incomplete. These three selections account for two key personnel working within the oncology group. It was further identified that the total salary allocation of approximately $177 thousand for a total of four key personnel in the oncology group for fiscal year ended September 30, 2024, lacked underlying support substantiating the amounts allocated to federal grants. • The SPA intake form includes key grant data and is used for updating indirect cost rates in the general ledger system. For one out of 12 selections of indirect costs, testing identified that the indirect cost rate in the accounting system was outdated. The SPA intake form was initiated for the indirect cost rate changes but was not internally submitted in a timely manner. Consequently, the actual indirect cost was allocated at a lower rate than authorized. • Documentation evidencing internal review of monthly labor distribution and budget to actual reports was not maintained. Additionally, this monthly review failed to detect key personnel whose effort form was not properly set up for certification purposes. Seven out of 120 special tests selections were identified to have missing effort forms. These seven selections represent three key personnel actively working on federal grants. Management further identified a total of 89 key personnel lacking effort forms, among which 37 key personnel have actively contributed efforts to federal awards. • For 20 out of 60 National Institute of Health salary cap selections related to special tests and provisions, the salary cap rate used for the calculation of salary cap for individual personnel was outdated and did not align with the authorized salary cap rate in the grant agreement. This results from ineffective review of grant budgets for updated rate information. These control deviations when considered in the aggregate are indicative of a significant deficiency in the design, implementation, and operating effectiveness of the internal controls. Questioned Costs—none New Finding—No, repeat finding reference number 2023-001 Cause—Personnel responsible for internal controls over compliance related to R&D were not adequately aware of the documentation requirements of Section 200.302-303. Additionally, the internal control framework is not clearly defined and relies heavily on manual control processes that were inconsistently implemented and documented. Reviews were not performed at a precise enough level and on a timely basis. Effect—Failures in internal controls have the potential to result in instances of noncompliance with R&D grant requirements. Recommendation— The deficiencies in internal controls identified during the audit related to R&D indicates that the controls over compliance for R&D should be assessed and, where necessary, corrective action needs to be taken to enable Baystate Health to produce appropriate supporting documentation on a timely basis and maintain appropriate internal controls over all compliance requirements. Specifically, we recommend that: • The roles and responsibilities of the individuals involved in the SPA should be challenged to ensure that all critical functions are addressed; the distribution of responsibilities is appropriate; and positions include an element of cross‐training. The capabilities of the individuals and the level of resources should be assessed to make sure that they are consistent with the responsibilities assigned. • Policies and procedures should be developed, documented and maintained/updated for all significant grant-related activities. On-going monitoring should take place to assure that such policies and procedures are executed accurately. Internal controls could be enhanced by standardizing best practices and providing ongoing training regarding federal requirements over compliance and documentation. • A system should be implemented to maintain documentation related to internal controls and compliance requirements for federal grants in such a way that this documentation is easily accessible and clearly interpretated. • The process for calculating and reviewing salary cap requirements should be revised to include a check that the reports reviewed as part of the control process are complete and accurate. • Controls should be implemented consistently to facilitate a timely review of indirect cost rates at the time of initial execution and revision of grant budgets within the general ledger.